Canonical Allele Identifier: CA2031026023
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363527G= , CM000674.2:g.40363527G= GRCh38
NC_000012.11:g.40757329G= , CM000674.1:g.40757329G= GRCh37
NC_000012.10:g.39043596G= NCBI36
NG_011709.1:g.143517G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7154G= MANE Select ENSP00000298910.7:p.Gly2385=
ENST00000636518.1:c.951G=
ENST00000679360.1:c.*6063G= ENSP00000505368.1:n.*6063G=
ENST00000679532.1:c.2928G=
ENST00000679683.1:c.944G=
ENST00000680018.1:c.2599G= ENSP00000505347.1:n.2599G=
ENST00000680422.1:c.4241G=
ENST00000680425.1:c.2321G= ENSP00000506459.1:n.2321G=
ENST00000680453.1:c.2611G=
ENST00000680790.1:c.6899G= ENSP00000505335.1:p.Gly2300=
ENST00000681136.1:n.3138G=
ENST00000681696.1:c.2837G= ENSP00000505871.1:p.Gly946=
ENST00000681773.1:n.361G=
ENST00000298910.11:c.7154G= ENSP00000298910.7:p.Gly2385=
ENST00000430804.5:c.4450G=
ENST00000479187.5:n.3835G=
NM_198578.3:c.7154G= NP_940980.3:p.Gly2385=
XM_005268629.2:c.7154G= XP_005268686.1:p.Gly2385=
XM_011537877.1:c.7154G= XP_011536179.1:p.Gly2385=
XM_011537879.1:c.5951G= XP_011536181.1:p.Gly1984=
XR_944868.1:n.485-8700C=
XM_005268629.4:c.7154G= XP_005268686.1:p.Gly2385=
XM_011537877.3:c.7154G= XP_011536179.1:p.Gly2385=
XM_017018787.1:c.4070G= XP_016874276.1:p.Gly1357=
XM_017018788.2:c.3416G= XP_016874277.1:p.Gly1139=
XM_024448833.1:c.5951G= XP_024304601.1:p.Gly1984=
XR_944868.2:n.485-8700C=
NM_198578.4:c.7154G= MANE Select NP_940980.4:p.Gly2385=